RESUMEN
Self-locomotion of liquid marbles, coated with lycopodium or fumed fluorosilica powder, filled with a saturated aqueous solution of camphor and placed on a water/vapor interface is reported. Self-propelled marbles demonstrated a complicated motion, representing a superposition of translational and rotational motions. Oscillations of the velocity of the center of mass and the angular velocity of marbles, occurring in the antiphase, were registered and explained qualitatively. Self-propulsion occurs because of the Marangoni solutocapillary flow inspired by the adsorption of camphor (evaporated from the liquid marble) by the water surface. Scaling laws describing translational and rotational motions are proposed and checked. The rotational motion of marbles arises from the asymmetry of the field of the Marangoni stresses because of the adsorption of camphor evaporated from marbles.
RESUMEN
Hierarchical metallic surfaces demonstrating pronounced water and oil repellence are reported. The surfaces were manufactured with stainless-steel microporous meshes, which were etched with perfluorononanoic acid. As a result, a hierarchical relief was created, characterized by roughness at micro- and sub-microscales. Pronounced superoleophobicity was registered with regard to canola, castor, sesame, flax, crude (petroleum), and engine oils. Relatively high sliding angles were recorded for 5 µL turpentine, olive, and silicone oil droplets. The stability of the Cassie-like air trapping wetting state, established with water/ethanol solutions, is reported. The omniphobicity of the surfaces is due to the interplay of their hierarchical relief and surface fluorination.
RESUMEN
This work investigated the influence of synthesis conditions, including the use of nonionic structure-forming compounds (surfactants) with different molecular weights (400-12,600 g/mol) and various hydrophilic/hydrophobic characteristics, as well as the use of a glass substrate and hydrothermal exposure on the texture and structural properties of ZnO samples. By X-ray analysis, it was determined that the synthesis intermediate in all cases is the compound Zn5(OH)8(NO3)2â2H2O. It was shown that thermolysis of this compound at 600 °C, regardless of the physicochemical properties of the surfactants, leads to the formation of ZnO with a wurtzite structure and spherical or oval particles. The particle size increased slightly as the molecular weight and viscosity of the surfactants grew, from 30 nm using Pluronic F-127 (MM = 12,600) to 80 nm using Pluronic L-31 (MM = 1100), PE-block-PEG (MM = 500) and PEG (MM = 400). Holding the pre-washed synthetic intermediates (Zn5(OH)8(NO3)2â2H2O) under hydrothermal conditions resulted in the formation of hexagonal ZnO rod crystal structures of various sizes. It was shown that the largest ZnO particles (10-15 µm) were observed in a sample obtained during hydrothermal exposure using Pluronic P-123 (MM = 5800). Atomic adsorption spectroscopy performed comparative quantitative analysis of residual Zn2+ ions in the supernatant of ZnO samples with different particle sizes and shapes. It was shown that the residual amount of Zn2+ ions was higher in the case of examining ZnO samples which have spherical particles of 30-80 nm. For example, in the supernatant of a ZnO sample that had a particle size of 30 nm, the quantitative content of Zn2+ ions was 10.22 mg/L.
RESUMEN
Textural and morphological features of hydrophobic silicon dioxide, obtained by the hydrolysis of tetraethoxysilane in an ammonia medium followed by modification of a spherical SiO2 particles surface with a hydrophobic polymethylhydrosiloxane, were studied in this work. The size of silicon dioxide particles was controlled during preparation based on the Stöber process by variation of the amount of water (mol) in relation to other components. The ratio of components, synthesis time and amount of the hydrophobizing agent were determined to obtain superhydrophobic monodisperse silicon dioxide with a spherical particle size of 50-400 nm and a contact angle of more than 150°. In the case of the struvite example, it was demonstrated that the application of spherical- shaped hydrophobic silicon dioxide particles in powder compounds significantly improves the flowability of crystalline hydrates. The functional additive based on the developed silicon dioxide particles makes it possible to implement the use of crystalline hydrates in fire-extinguishing powders, preventing agglomeration and caking processes. The high fire-extinguishing efficiency of the powder composition based on struvite and the developed functional additive has been proven by using thermal analysis methods (TGA/DSC).
RESUMEN
Interfacial crystallization appears as a crucial stage in the numeral natural phenomena and technological applications, such as industry of semi-conductors and manufacturing of nano-whiskers. Interfacial aspects of heterogeneous crystallization are surveyed. The review is focused on the interplay of thermodynamic and geometric aspects of the interfacial crystallization. Thermodynamic considerations leading to the Wulff construction are discussed. Equilibrium shape of the crystallized particle in the contact with a foreign substrate giving rise to the Winterbottom construction is treated. The concept of equivalent equilibrium contact angle θeq is introduced. The equivalent contact angle θeq applicable for isotropic crystals does not depend neither on the volume of the crystallized particles nor on the external fields. Bulk contributions to the free energy of the particle such as the bulk heat release in the case of reactive contact or latent heat of crystallization do not influence the equivalent contact angle θeq. Application of the Winterbottom constructions for prediction of the shape of nanoparticles grown on solid substrates is treated. Thermodynamics of interfacial crystallization is discussed. The thermodynamic condition predicting when surface crystallization is thermodynamically favored over homogeneous (bulk) crystallization is supplied. This thermodynamic relation coincides with the condition prescribing the partial wetting of a solid by its melt. Interfacial crystallization in its relation to the "coffee-stain" effect, salt creeping and development of anti-icing surfaces is addressed. Interfacial aspects of epitaxial growth of crystals are considered. The current state-of-art in the field is reviewed.
RESUMEN
Omniphobic and icephobic twin-scale surfaces based on the "urchin"-like fluorinated Al2O3 particles are presented. Combined effect of hierarchical topography and fluorination supplied to the surfaces omniphobic and icephobic properties. The study of the stability of the Cassie wetting state is reported. High apparent contact angles were accompanied with the low contact angle hysteresis and high stability of the Cassie air trapping wetting state. Time delay of the ice crystallization as high as [Formula: see text] min was established when compared to the ice formation on flat aluminum and non-fluorinated "urchin"-like surfaces. Crystallized water droplets formed on the reported nano-structured surfaces were easily blown out by the air jet with the velocity of [Formula: see text] m/s, (which is markedly lower than that common for exploitation of aircrafts and turbines). Heated "urchin"-like surfaces completely restored their omniphobic and icephobic surfaces after thawing. Qualitative analysis of water freezing is supplied.
RESUMEN
Using a developed co-precipitation method, we synthesized spherical Fe3O4 nanoparticles with a wide nonlinear absorption band of visible radiation. Optical properties of the synthesized nanoparticles dispersed in an optically transparent copolymer of methyl methacrylate with styrene were studied by optical spectroscopy and z-scan techniques. We found that the electric polarizability of Fe3O4 nanoparticles is altered by low-intensity visible radiation (I ≤ 0.2 kW/cm2; λ = 442 and 561 nm) and reaches a value of 107 Å3. The change in polarizability is induced by the intraband phototransition of charge carriers. This optical effect may be employed to improve the drug uptake properties of Fe3O4 nanoparticles. PACS: 33.15.Kr78.67.Bf42.70.Nq.